Primary Site >> Pancreatic Cancer

Gene >> PCDH10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151373:133151373(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1233T>G
AA Mutation p.Asn411Lys(p.N411K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151918:133151918(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771704218
CDS Mutation c.1778C>T
AA Mutation p.Ser593Leu(p.S593L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133152184:133152184(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2044G>A
AA Mutation p.Ala682Thr(p.A682T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133163016:133163016(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2837C>A
AA Mutation p.Ala946Asp(p.A946D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264360
Start 133151716:133151716(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1576T>G
AA Mutation p.Tyr526Asp(p.Y526D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000264360
Start 133152051:133152051(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1911G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000264360
Start 133150759:133150759(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.619G>T
AA Mutation p.Gly207Ter(p.G207*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript